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机译:Lgi1空突变小鼠表现出肌阵挛性发作和CA1神经元过度兴奋
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY 14263, USA;
Institute of Molecular Medicine and Genetics, and Department of Neurology, Medical College of Georgia, Augusta, GA 30912, USA and;
MCG Cancer Center, School of Medicine and;
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY 14263, USA;
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY 14263, USA;
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY 14263, USA;
Department of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, NY 14263, USA;
Institute of Molecular Medicine and Genetics, and Department of Neurology, Medical College of Georgia, Augusta, GA 30912, USA and;
机译:Lgi1空突变小鼠表现出肌阵挛性发作和CA1神经元过度兴奋。
机译:异常的神经元模式发生在Scn1b-null小鼠的出生后早期大脑发育过程中,并在过度兴奋之前
机译:脑源性神经营养因子转基因小鼠表现出被动回避缺陷,癫痫发作严重程度增加以及海马和内嗅皮层的体外过度兴奋性。
机译:神经元死亡机制:在柔软突变小鼠中的体内研究
机译:年轻的铜蓝蛋白敲除小鼠表现出神经元脆弱性增加和焦虑增加:铁和BDNF的作用。
机译:Lgi1空突变小鼠表现出肌阵挛性发作和CA1神经元过度兴奋
机译:Lgi1空突变小鼠表现出肌阵挛性发作和CA1神经元过度兴奋